A Hybrid G-Quadruplex Structure Formed by a Sequence from the MAX Gene

Here, we report the NMR solution structure of the G-quadruplex (G4) folded by the 24-nt guanine-rich DNA sequence d-[AG<sub>3</sub>AG<sub>4</sub>A<sub>2</sub>G<sub>4</sub>TGA<sub>2</sub>G<sub>4</sub>A]. The sequence is originated from the first intron of the MAX gene, which encodes the transcription factor MAX, an obligate partner of the notorious oncoprotein MYC. The unimolecular G4 adopts a [3 + 1] hybrid topology containing all the three main loop types (propeller, diagonal, and lateral). Also, the three G-tetrads are stacked with the same polarity of the Hoogsteen hydrogen bond and <i>anti</i>-<i>anti</i>-<i>anti</i>-<i>syn</i> glycosidic configuration pattern. Both 5' and 3'-flanking regions contain one adenine residue. As far as we know, it is the first example of such a unique topology wherein all the nucleotides are not modified in either sugars or bases. In addition to the well-defined G-tetrad core, the diagonal loop contains a G·(A-G) triad, and a T·G base pair is formed within the lateral loop. Furthermore, the formation of the G4 is found to be stable under physiological conditions even without annealing and acts as a barrier to DNA polymerase. These findings provided deep insights into the G4 folding topology and a potential for targeting MAX G4.

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Publication Details

Journal
JACS Au
Published
2025-11-06
DOI
https://doi.org/10.1021/jacsau.5c01247
Primary Topic
DNA and Nucleic Acid Chemistry
Type
article
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article

A Hybrid G-Quadruplex Structure Formed by a Sequence from the MAX Gene

Xiao Hu, Ni Xiao, Wenxian Lan, Chunyang Cao
JACS Au
DNA and Nucleic Acid Chemistry
article

A Hybrid G-Quadruplex Structure Formed by a Sequence from the MAX Gene

Xiao Hu, Ni Xiao, Wenxian Lan, Chunyang Cao
article en

Abstract

Here, we report the NMR solution structure of the G-quadruplex (G4) folded by the 24-nt guanine-rich DNA sequence d-[AG<sub>3</sub>AG<sub>4</sub>A<sub>2</sub>G<sub>4</sub>TGA<sub>2</sub>G<sub>4</sub>A]. The sequence is originated from the first intron of the MAX gene, which encodes the transcription factor MAX, an obligate partner of the notorious oncoprotein MYC. The unimolecular G4 adopts a [3 + 1] hybrid topology containing all the three main loop types (propeller, diagonal, and lateral). Also, the three G-tetrads are stacked with the same polarity of the Hoogsteen hydrogen bond and <i>anti</i>-<i>anti</i>-<i>anti</i>-<i>syn</i> glycosidic configuration pattern. Both 5' and 3'-flanking regions contain one adenine residue. As far as we know, it is the first example of such a unique topology wherein all the nucleotides are not modified in either sugars or bases. In addition to the well-defined G-tetrad core, the diagonal loop contains a G·(A-G) triad, and a T·G base pair is formed within the lateral loop. Furthermore, the formation of the G4 is found to be stable under physiological conditions even without annealing and acts as a barrier to DNA polymerase. These findings provided deep insights into the G4 folding topology and a potential for targeting MAX G4.

JACS AuVol. 5(11)
Chinese Academy of Sciences (CN), Shanghai Institute of Organic Chemistry (CN), Center for Excellence in Molecular Plant Sciences (CN), State Key Laboratory of Chemical Engineering (CN)
Openalex Percentile: Top 71%
DNA and Nucleic Acid Chemistry
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